Dvortsin Evgeni, Gout-Zwart Judith, Eijssen Ernst-Lodewijk Marie, van Brussel Jan, Postma Maarten J
Department of Pharmacy, Unit of PharmacoEpidemiology and PharmacoEconomics (PE2), University of Groningen, Groningen, The Netherlands.
University Medical Center Groningen (UMCG), Institute of Science in Healthy Aging & healthcaRE (SHARE), University of Groningen, Groningen, The Netherlands.
PLoS One. 2016 Jan 22;11(1):e0146551. doi: 10.1371/journal.pone.0146551. eCollection 2016.
Many oncological drugs that are being used in the adjuvant setting were first submitted for reimbursement in the metastatic stage, with differences in incremental cost-effectiveness ratios (ICERs) in both settings having potential implications for reimbursement and pricing. The aim of this study is to identify a possible trend in the cost-effectiveness for the early/adjuvant and late/metastatic stages of oncological drugs through review and case study.
We reviewed pairs of cost-effectiveness analyses of the same oncological drug in different stages for Scotland and the Netherlands. The case study in this report was directed at trastuzumab in the Dutch situation. Using a simplified Markov model, the cost-effectiveness in early and late stage of breast cancer was calculated and compared to the findings from the review.
Comparable studies were found for cetuximab, bortezomib and bosutinib. Treatments in the late stage were found to be more expensive per QALY by a factor ranging from 1.5 to 12. The case study provided a similar result; late stage treatment was more expensive by a factor 10. Using, for example, a threshold of € 80,000/QALY, the early stage of cetuximab, bosutinib and trastuzumab are deemed cost-effective, while their compared late stage is lifted over the threshold and potentially considered not cost-effective.
ICERs of oncological drugs used in different stages are more unfavourable in the late stage than in the early stage. Applying a reasonable threshold may result in early stage treatment being deemed cost-effective while late stage potentially not. Authorities should be aware of this when assessing oncological drugs and interpreting the corresponding ICERs, in the situation where oncological drugs are generally most submitted for reimbursement in the late stage initially.
许多用于辅助治疗的肿瘤药物最初是在转移性阶段提交报销申请的,两种情况下的增量成本效益比(ICER)差异对报销和定价可能产生影响。本研究的目的是通过综述和案例研究,确定肿瘤药物在早期/辅助阶段和晚期/转移性阶段成本效益的可能趋势。
我们回顾了苏格兰和荷兰针对同一种肿瘤药物在不同阶段的成本效益分析对。本报告中的案例研究针对荷兰情况下的曲妥珠单抗。使用简化的马尔可夫模型,计算了乳腺癌早期和晚期的成本效益,并与综述结果进行比较。
发现了西妥昔单抗、硼替佐米和博舒替尼的可比研究。发现晚期治疗每获得一个质量调整生命年(QALY)的成本要高出1.5至12倍。案例研究提供了类似的结果;晚期治疗成本高出10倍。例如,使用80,000欧元/QALY的阈值,西妥昔单抗、博舒替尼和曲妥珠单抗的早期阶段被认为具有成本效益,而与之相比的晚期阶段则超过了阈值,可能被认为不具有成本效益。
不同阶段使用的肿瘤药物的ICER在晚期比早期更不理想。应用合理的阈值可能导致早期治疗被认为具有成本效益,而晚期治疗可能不具有成本效益。在评估肿瘤药物并解释相应的ICER时,当局应意识到这一点,因为肿瘤药物通常最初大多是在晚期提交报销申请的。